Knowledge of Microsoft® Office;
Excellent organization and communication skills;
Great attention to detail.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
Office based environment with on-site mentors
Defined career paths with clear advancement opportunities
Industry renowned onboarding and training programs designed to accelerate professional development
Ongoing training and continuous learning opportunities throughout your career
An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
Competitive compensation programs that recognize and reward performance
Comprehensive health, wellness, retirement, and PTO benefits
Office based culture with occasional WFH that provides flexibility for eligible positions after training
Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Provide day-to-day departmental support activities to Regulatory Submissions Coordinators;
Maintain database and spreadsheets as necessary to facilitate tracking and documentation of departmental activities;
Collect, review, organize, and assemble regulatory start-up submissions; and,
Perform other tasks as needed.
Additional Responsibilities
Prepare, review, and file clinical trial applications
Communicate with research sites (hospitals, etc.) to collect all essential documents required before the site starts to enrol patients to participate in the clinical trial;
Provide insightful input on regulatory submissions documents and maintain timelines for study start-up through both internal and external collaboration;
Ensure submissions comply with applicable regulations and guidance documents.
Bachelor's degree in a Life Sciences field;
At least 2 years of work experience as a Regulatory Submissions Coordinator;
Hands-on experience preparing, reviewing, and submitting regulatory documentation;
Knowledge of Microsoft® Office;
Excellent organization and communication skills;
Great attention to detail.
